R01AA029113
Project Grant
Overview
Grant Description
Prazosin Treatment for Alcohol Use Disorder with Alcohol Withdrawal Symptoms - Project Abstract
Alcohol Use Disorder (AUD) is a chronic relapsing illness in which Alcohol Withdrawal Symptoms (AW) are associated with greater treatment failure risk and higher rates of relapse and alcohol intake. Efficacy of current approved medications in AUD are modest, and none have been shown to be efficacious in those with AW. Thus, there is great need to develop and evaluate treatments to address specific prognostic indicators of high relapse and treatment failure to reduce the associated burden of AUD.
Based on this previous clinical research, we hypothesized that in AUD patients with AW (AUD+AW), PR (16 mg/day) compared to PBO will significantly improve alcohol use outcomes, craving, and also reduce associated anxiety and depression symptoms and improve physical health (SBP and liver enzymes) functioning and patient-related outcomes during the course of the trial and with enduring effects during over a 3-month follow-up period, thereby validating AW as a prognostic indicator both of prazosin efficacy and in AUD treatment outcome.
A 12-week Phase II, single-site, randomized clinical trial of prazosin (PR: 16 mg/day, T.I.D dosing) is proposed in 150 treatment-seeking men and women with AUD+AW (3 or more symptoms) to address the following specific aims:
Aim #1: To evaluate the effects of PR vs PBO on the primary alcohol use outcome of percent of subjects with no heavy drinking day (PSNHDD) and secondary drinking outcomes of %heavy drinking day (HDD%), any drinking day (DD%), and average drinks/day (AVGD) in AUD+AW patients.
Aim #2: To assess the effects of PR vs PBO on other secondary stress-related outcomes of alcohol craving, depression, and anxiety symptoms during the trial.
Aim #3: To assess enduring short-term treatment effects of PR versus PBO on primary and other secondary outcomes at 1- and 3-month post-treatment follow-up time points.
Exploratory Aim 1: To assess the effects of PR vs PBO treatment during the trial and at follow-up on secondary physical health (SBP/DBP and liver enzymes) and patient-reported functioning outcomes.
Exploratory Aim 2: To explore whether pre-treatment patient characteristics (gender, adversity/trauma history, and lifetime PTSD) influence prazosin effects on primary and secondary alcohol use and related outcomes.
Prazosin is a commonly prescribed medication that most clinicians feel comfortable using. If successful, findings will provide important efficacy data on prazosin's role in AUD+AW treatment and in related secondary psychological and physical health outcomes. It will further validate AW at outpatient treatment entry as a prognostic indicator for AUD treatment and for prazosin use among AUD+AW subgroup of patients. It will also support the development of the precision medicine goal of providing specific treatment options for AUD patients with AW and stress-related pathophysiology to improve their AUD treatment outcomes.
Alcohol Use Disorder (AUD) is a chronic relapsing illness in which Alcohol Withdrawal Symptoms (AW) are associated with greater treatment failure risk and higher rates of relapse and alcohol intake. Efficacy of current approved medications in AUD are modest, and none have been shown to be efficacious in those with AW. Thus, there is great need to develop and evaluate treatments to address specific prognostic indicators of high relapse and treatment failure to reduce the associated burden of AUD.
Based on this previous clinical research, we hypothesized that in AUD patients with AW (AUD+AW), PR (16 mg/day) compared to PBO will significantly improve alcohol use outcomes, craving, and also reduce associated anxiety and depression symptoms and improve physical health (SBP and liver enzymes) functioning and patient-related outcomes during the course of the trial and with enduring effects during over a 3-month follow-up period, thereby validating AW as a prognostic indicator both of prazosin efficacy and in AUD treatment outcome.
A 12-week Phase II, single-site, randomized clinical trial of prazosin (PR: 16 mg/day, T.I.D dosing) is proposed in 150 treatment-seeking men and women with AUD+AW (3 or more symptoms) to address the following specific aims:
Aim #1: To evaluate the effects of PR vs PBO on the primary alcohol use outcome of percent of subjects with no heavy drinking day (PSNHDD) and secondary drinking outcomes of %heavy drinking day (HDD%), any drinking day (DD%), and average drinks/day (AVGD) in AUD+AW patients.
Aim #2: To assess the effects of PR vs PBO on other secondary stress-related outcomes of alcohol craving, depression, and anxiety symptoms during the trial.
Aim #3: To assess enduring short-term treatment effects of PR versus PBO on primary and other secondary outcomes at 1- and 3-month post-treatment follow-up time points.
Exploratory Aim 1: To assess the effects of PR vs PBO treatment during the trial and at follow-up on secondary physical health (SBP/DBP and liver enzymes) and patient-reported functioning outcomes.
Exploratory Aim 2: To explore whether pre-treatment patient characteristics (gender, adversity/trauma history, and lifetime PTSD) influence prazosin effects on primary and secondary alcohol use and related outcomes.
Prazosin is a commonly prescribed medication that most clinicians feel comfortable using. If successful, findings will provide important efficacy data on prazosin's role in AUD+AW treatment and in related secondary psychological and physical health outcomes. It will further validate AW at outpatient treatment entry as a prognostic indicator for AUD treatment and for prazosin use among AUD+AW subgroup of patients. It will also support the development of the precision medicine goal of providing specific treatment options for AUD patients with AW and stress-related pathophysiology to improve their AUD treatment outcomes.
Awardee
Funding Goals
TO DEVELOP A SOUND FUNDAMENTAL KNOWLEDGE BASE WHICH CAN BE APPLIED TO THE DEVELOPMENT OF IMPROVED METHODS OF TREATMENT AND MORE EFFECTIVE STRATEGIES FOR PREVENTING ALCOHOLISM AND ALCOHOL-RELATED PROBLEMS. THE NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM (NIAAA) SUPPORTS RESEARCH IN A BROAD RANGE OF DISCIPLINES AND SUBJECT AREAS RELATED TO BIOMEDICAL AND GENETIC FACTORS, PSYCHOLOGICAL AND ENVIRONMENTAL FACTORS, ALCOHOL-RELATED PROBLEMS AND MEDICAL DISORDERS, HEALTH SERVICES RESEARCH, AND PREVENTION AND TREATMENT RESEARCH. SMALL BUSINESS INNOVATION RESEARCH (SBIR) PROGRAM: TO INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT, TO INCREASE SMALL BUSINESS PARTICIPATION IN FEDERAL RESEARCH AND DEVELOPMENT, AND TO FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN TECHNOLOGICAL INNOVATION. SMALL BUSINESS TECHNOLOGY TRANSFER (STTR) PROGRAM: TO STIMULATE AND FOSTER SCIENTIFIC AND TECHNOLOGICAL INNOVATION AND TECHNOLOGY TRANSFER THROUGH COOPERATIVE RESEARCH AND DEVELOPMENT CARRIED OUT BETWEEN SMALL BUSINESS CONCERNS AND RESEARCH INSTITUTIONS, TO INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT, AND TO FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN TECHNOLOGICAL INNOVATION.
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
New Haven,
Connecticut
065191717
United States
Geographic Scope
Single Zip Code
Related Opportunity
Analysis Notes
Amendment Since initial award the total obligations have increased 384% from $747,658 to $3,615,761.
Yale Univ was awarded
Effective Prazosin Treatment Alcohol Use Disorder with Withdrawal Symptoms
Project Grant R01AA029113
worth $3,615,761
from National Institute on Alcohol Abuse and Alcoholism in May 2021 with work to be completed primarily in New Haven Connecticut United States.
The grant
has a duration of 4 years 9 months and
was awarded through assistance program 93.273 Alcohol Research Programs.
The Project Grant was awarded through grant opportunity Research Project Grant (Parent R01 Clinical Trial Required).
Status
(Ongoing)
Last Modified 5/5/25
Period of Performance
5/15/21
Start Date
2/28/26
End Date
Funding Split
$3.6M
Federal Obligation
$0.0
Non-Federal Obligation
$3.6M
Total Obligated
Activity Timeline
Transaction History
Modifications to R01AA029113
Additional Detail
Award ID FAIN
R01AA029113
SAI Number
R01AA029113-3029003653
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Private Institution Of Higher Education
Awarding Office
75N500 NIH National Institute on Alcohol Abuse and Alcoholism
Funding Office
75N500 NIH National Institute on Alcohol Abuse and Alcoholism
Awardee UEI
FL6GV84CKN57
Awardee CAGE
4B992
Performance District
CT-03
Senators
Richard Blumenthal
Christopher Murphy
Christopher Murphy
Budget Funding
Federal Account | Budget Subfunction | Object Class | Total | Percentage |
---|---|---|---|---|
National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Health and Human Services (075-0894) | Health research and training | Grants, subsidies, and contributions (41.0) | $1,452,113 | 100% |
Modified: 5/5/25